(Q24294333)

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Replacement of charged and polar residues in the coiled-coiled interface of huntingtin-interacting protein 1 (HIP1) causes aggregation and cell death

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Replacement of charged and polar residues in the coiled-coiled interface of huntingtin-interacting protein 1 (HIP1) causes aggregation and cell death (English)

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Sarah N Fontaine

1

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Scott P Bauer

2

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Xiaoyan Lin

3

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Sara Poorfarahani

4

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Joel A Ybe

5

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language of work or name

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publication date

21 September 2012

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586

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3030-6

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19

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HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

The Sla2p/HIP1/HIP1R family: similar structure, similar function in endocytosis?

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

The design of coiled-coil structures and assemblies

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

The role of position a in determining the stability and oligomerization state of alpha-helical coiled coils: 20 amino acid stability coefficients in the hydrophobic core of proteins

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Conformation Switching of Clathrin Light Chain Regulates Clathrin Lattice Assembly

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Crystal Structure at 2.8 Å of Huntingtin-Interacting Protein 1 (HIP1) Coiled-Coil Domain Reveals a Charged Surface Suitable for HIP1 Protein Interactor (HIPPI)

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Crystal Structure at 2.8 Å of the DLLRKN-containing Coiled-coil Domain of Huntingtin-interacting Protein 1 (HIP1) Reveals a Surface Suitable for Clathrin Light Chain Binding

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

K2D2: estimation of protein secondary structure from circular dichroism spectra.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

HIP1 functions in clathrin-mediated endocytosis through binding to clathrin and adaptor protein 2

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Huntingtin interacting protein 1 induces apoptosis via a novel caspase-dependent death effector domain

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Huntingtin-interacting protein 1-mediated neuronal cell death occurs through intrinsic apoptotic pathways and mitochondrial alterations

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Regulation of the proapoptotic activity of huntingtin interacting protein 1 by Dyrk1 and caspase-3 in hippocampal neuroprogenitor cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Cell-produced alpha-synuclein oligomers are targeted to, and impair, the 26S proteasome

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

The E693Delta mutation in amyloid precursor protein increases intracellular accumulation of amyloid beta oligomers and causes endoplasmic reticulum stress-induced apoptosis in cultured cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Oligomers of mutant glial fibrillary acidic protein (GFAP) Inhibit the proteasome system in alexander disease astrocytes, and the small heat shock protein alphaB-crystallin reverses the inhibition

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Disease-associated prion protein oligomers inhibit the 26S proteasome

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Disease-associated amyloid and misfolded protein aggregates activate the inflammasome

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Protein aggregation diseases: toxicity of soluble prefibrillar aggregates and their clinical significance

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Essential role of coiled coils for aggregation and activity of Q/N-rich prions and PolyQ proteins

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.07.011

21 January 2018

Identifiers

10.1016/J.FEBSLET.2012.07.011

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release_wevwy4bzwbbr3jlcnsx4dprcta

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